US4369124A - High viscosity complexed aqueous gels and methods and additives for forming such gels - Google Patents

High viscosity complexed aqueous gels and methods and additives for forming such gels Download PDF

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US4369124A
US4369124A US06/075,481 US7548179A US4369124A US 4369124 A US4369124 A US 4369124A US 7548179 A US7548179 A US 7548179A US 4369124 A US4369124 A US 4369124A
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hydroxy
monomers
complexing agent
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Eugene A. Elphingstone
John M. Dees
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Halliburton Co
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Halliburton Co
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Priority to AU58792/80A priority patent/AU5879280A/en
Priority to GB8018337A priority patent/GB2058750A/en
Priority to NO801679A priority patent/NO801679L/en
Priority to NL8003501A priority patent/NL8003501A/en
Priority to BR8004199A priority patent/BR8004199A/en
Priority to IT24638/80A priority patent/IT1141046B/en
Priority to DE19803034721 priority patent/DE3034721A1/en
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/84Compositions based on water or polar solvents
    • C09K8/86Compositions based on water or polar solvents containing organic compounds
    • C09K8/88Compositions based on water or polar solvents containing organic compounds macromolecular compounds
    • C09K8/90Compositions based on water or polar solvents containing organic compounds macromolecular compounds of natural origin, e.g. polysaccharides, cellulose
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G79/00Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0091Complexes with metal-heteroatom-bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/56Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L35/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/52Compositions for preventing, limiting or eliminating depositions, e.g. for cleaning
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/62Compositions for forming crevices or fractures
    • C09K8/72Eroding chemicals, e.g. acids
    • C09K8/74Eroding chemicals, e.g. acids combined with additives added for specific purposes
    • C09K8/76Eroding chemicals, e.g. acids combined with additives added for specific purposes for preventing or reducing fluid loss
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/84Compositions based on water or polar solvents
    • C09K8/86Compositions based on water or polar solvents containing organic compounds
    • C09K8/88Compositions based on water or polar solvents containing organic compounds macromolecular compounds
    • C09K8/882Compositions based on water or polar solvents containing organic compounds macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds

Definitions

  • High viscosity aqueous gels containing hydrated organic polymers crosslinked or complexed by metal containing complexing agents have been developed heretofore.
  • Such complex aqueous gels have a variety of uses including, but not limited to, suspending explosive materials used in mining, drilling and other similar applications, carrying out production stimulation procedures in oil, gas and water wells, carrying out subterranean well completions, transporting proppant or other materials into desired areas in subterranean well formations, diverting fluids in subterranean well formations, and carrying out cleaning procedures such as in cleaning of tubular goods, production equipment and industrial equipment.
  • High viscosity aqueous gels are particularly suitable as treating fluids in carrying out subterranean well formation acidizing, fracturing and fracture acidizing procedures.
  • the high viscosity of the treating fluids prevents acid therein from becoming prematurely spent and inactive, enables the development of wider fractures in fracturing and fracture acidizing procedures, permits better fluid loss control and increases the proppant or other particulated material carrying capacity of the treating fluids.
  • Hydrophilic organic polymers such as hydratable polysaccharides and hydratable synthetic polymers, e.g., polyacrylamide, have been widely used to form aqueous gels.
  • Numerous solid metallic crosslinking or complexing agents have also been employed to complex the hydrated gelling agents thereby forming a highly viscous aqueous fluid.
  • the metallic complexing agents used heretofore include antimony salts, aluminum salts, chromium salts, and certain organic titanates.
  • all of such complexing agents are limited in their use in that specific conditions of pH, temperature, other chemicals, etc. are required for the complexing reaction between the complexing agent and the hydrated organic polymers utilized to take place.
  • antimony complexing agents require that the aqueous gel have a specific pH and temperature before the complexing reaction takes place.
  • Other metallic complexing agents such as chromium salts require oxidation-reduction for crosslinking.
  • heretofore used complexing agents require separate mixing with the aqueous gel formed after the hydrated organic polymer or polymers utilized have been hydrated thereby requiring the use of elaborate mixing procedures and equipment for preparing the desired high viscosity complexed aqueous gels.
  • a solid crystalline complexing agent which reacts with aqueous gels containing hydrated organic polymers such as polysaccharides and polyacrylamides to form the aqueous gel into a high viscosity complexed aqueous fluid over a broad range of pH and temperature conditions.
  • solid additives are provided containing one or more hydratable organic polymers and the aforesaid complexing agent which can be combined directly with an aqueous fluid to form a highly viscous complexed aqueous gel at a desired pH and/or temperature.
  • High viscosity complexed aqueous gels and methods of forming such gels utilizing the complexing agents and additives of this invention are also provided.
  • the complexing agents of this invention are solid crystalline materials comprised of organic titanate monomers, homopolymers of such monomers and mixtures of such monomers and homopolymers, the monomers having the following general formula:
  • R 1 is a bidentate organic ligand having one covalent bond and one coordinate covalent bond and having from 2 to 18 carbon atoms selected from the group consisting of ⁇ , ⁇ and ⁇ hydroxy acids, ⁇ , ⁇ and ⁇ hydroxy esters, ⁇ , ⁇ and ⁇ hydroxy aldehydes, ⁇ , ⁇ and ⁇ hydroxy ketones, ⁇ , ⁇ and ⁇ hydroxy ethers, ⁇ , ⁇ and ⁇ sulfur containing groups, and ⁇ , ⁇ and ⁇ amines;
  • R 2 is a monodentate organic ligand having from 1 to 18 carbon atoms selected from the group consisting of alkoxy, aryloxy and other hydroxy organic groups;
  • w is an integer in the range of from 1 to 4;
  • y is 0 or an integer in the range of from 1 to 3;
  • z is 0 or an integer in the range of from 1 to 3.
  • R 1 ligands which can be present in the organic titanate monomer are 2,2',2" nitrilodiethanol monoethoxide, acetylacetone-enolate and ammonium propanate-2-oxide.
  • R 2 groups which can be present in the monomer are methoxy, ethoxy, propoxy, isopropoxy, butoxy, phenoxy and octadecoxy. Of these, methoxy, butoxy and isopropoxy are preferred with isopropoxy being the most preferred.
  • a more preferred complexing agent of the present invention is a solid crystalline material comprised of organic titanate monomers, homopolymers of such monomers and mixtures of such monomers and homopolymers, the monomers having the general formula:
  • R 1 is a group of the type described above; w is an integer of from 1 to 2; y is 0 to 3; and z is 0 to 3.
  • monomers are titanium bis [2,2',2" nitrilodiethanol monoethoxide] dihydroxide, titanium bis acetylacetone-enolate dihydroxide, and titanium bis [ ammonium propanate-2-oxide] dihydroxide. Of these, titanium bis acetylacetone-enolate dihydroxide is the most preferred.
  • the most preferred complexing agent of the present invention is comprised of an organic titanate monomer, homopolymers of such monomer and mixtures thereof wherein said monomer is titanium bis acetylacetone-enolate dihydroxide.
  • the solid crystalline complexing agents of this invention can be prepared in various ways.
  • a tetra-alkoxy titanate can be reacted with an organic ketone, ester, amine or alcohol to produce a reaction product which when hydrolyzed forms the solid crystalline organic titanate complexing agent of this invention.
  • titanium (IV) tetraisopropoxide can be reacted with acetylacetone in a 1:2 mole ratio to form titanium bis acetylacetone-enolate bis isopropoxide.
  • This reaction product can then be combined with excess water at room temperature with moderate agitation to yield the organic titanate complexing agent of this invention as a precipitate. When dried, the precipitate is a white to yellow powder, crystalline in nature.
  • An alternate procedure which can be utilized to form the organic titanate complexing agents of this invention is to react a titanium tetrahalide with an organic acetone, acetate, amine or alcohol in the presence of water and a base.
  • titanium tetrachloride can be reacted with acetylacetone in a 1:1 mole ratio in excess water and a base for neutralization to form the solid organic titanate.
  • the complexing agents of this invention react with hydrated gelling agents to complex such gelling agents and form a highly viscous complexed aqueous gel over a broad pH and temperature range, i.e., at a pH in the range of from about 3 to about 12 and at a temperature in the range of from about 40° F. to about 400° F., and preferably up to about 100° to 120° F.
  • Solid hydratable gelling agents which are preferred for use in accordance with this invention are hydratable polysaccharides and hydratable synthetic polymers such as polyacrylamides. Particularly preferred hydratable polysaccharides are gelactomannan gums and derivatives thereof, glucomannan gums and derivatives thereof, and cellulose derivatives.
  • guar gum examples include guar gum, locust bean gum, karaya gum, sodium carboxymethylguar, hydroxyethylguar, sodium carboxymethylhydroxyethylguar, hydroxypropylguar, sodium carboxymethylhydroxypropylcellulose, sodium carboxyethylhydroxyethylcellulose, and hydroxyethylcellulose.
  • the hydroxyethylcellulose derivative used as gelling agents should be those having between 0.5 and about 10 moles of ethylene oxide per anhydroglucose unit.
  • the most preferred gelling agent for use in accordance with this invention is hydroxypropylguar.
  • the complexing agent of this invention is a crystalline material of fine particle size, it can be uniformly mixed with one or more of the solid gelling agents described above to form a solid powder additive which can be combined directly with an aqueous fluid, either in a batch or continuous process, to form a highly viscous complexed aqueous gel.
  • the organic titanate complexing agent is dissolved in aqueous fluids at a slower rate than the gelling agents described above thereby allowing the gelling agents to hydrate prior to being complexed by the complexing agent when the gelling agent and complexing agent are added to an aqueous fluid simultaneously.
  • the additives of this invention for forming high viscosity complexed aqueous gels can include a variety of other solid chemicals to bring about desired results.
  • breakers for the complexed gels produced by the additives can be included in the additives such as oxidizing agents, enzymes, acids and mixtures of such compounds.
  • particularly suitable oxidizing agents are sodium persulfate and ammonium persulfate.
  • Suitable enzymes which can be used are ⁇ and ⁇ amylases, amyloglucosidase, aligoglucosidase, invertase, maltase, cellulase and hemicellulase.
  • An example of a suitable acid is fumaric acid. Of these, a mixture of sodium persulfate, hemicellulase and cellulase is perferred.
  • Other solid additives such as buffers, surface active agents, fluid loss control chemicals, etc., can also be included.
  • R 1 is a bidentate organic ligand having one covalent bond and one coordinate covalent bond and having from 2 to 18 carbon atoms selected from the group consisting of ⁇ , ⁇ and ⁇ hydroxy acids, ⁇ , ⁇ and ⁇ hydroxy ketones, ⁇ , ⁇ and ⁇ hydroxy ethers and ⁇ , ⁇ and ⁇ hydroxy sulfur containing groups;
  • R 2 is a monodentate organic ligand having from 1 to 18 carbon atoms selected from the group consisting of alkoxy, aryloxy and other hydroxy organic groups;
  • w is an integer in the range of from 1 to 4;
  • x is 0 or an integer in the range of from 1 to 3;
  • y is 0 or an integer in the range of from 1 to 3;
  • z is 0 or an integer in the range of from 1 to 3.
  • a more preferred additive of this invention is comprised of a mixture of a solid gelling agent selected from the group consisting of sodium carboxymethylhydroxyethylcellulose, guar, hydroxypropylguar, hydratable polyacrylamide and mixtures thereof, and a solid complexing agent comprised of organic titanate monomers, homopolymers and mixtures of such monomers and homopolymers, the monomers having the following general formula:
  • R 1 is a bidentate organic ligand having one covalent bond and one coordinate covalent bond and having from 2 to 18 carbon atoms selected from the group consisting of ⁇ , ⁇ and ⁇ hydroxy acids, ⁇ , ⁇ and ⁇ hydroxy esters, ⁇ , ⁇ and ⁇ hydroxy aldehydes, ⁇ , ⁇ and ⁇ hydroxy ketones and ⁇ , ⁇ and ⁇ hydroxy ethers, and ⁇ , ⁇ and ⁇ hydroxy sulfur containing groups;
  • w is an integer from 1 to 2;
  • y is 0 to 3;
  • z is 0 to 3.
  • the most preferred additive of this invention comprises a mixture of solid hydroxypropylguar gelling agent and a solid complexing agent comprised of an organic titanate monomer, homopolymers of such monomer and mixtures thereof wherein said monomer is titanium bis acetylacetone-enolate dihydroxide.
  • the solid additives of this invention for forming highly viscous complexed aqueous gels when combined with an aqueous fluid preferably include complexing agent and gelling agent in amounts whereby the weight ratio of complexing agent to gelling agent is in the range of from about 0.01 to about 0.20.
  • a more preferred additive contains complexing agent to gelling agent in a weight ratio in the range of from about 0.02 to about 0.10, and the most preferred additive contains complexing agent to gelling agent in a weight ratio of 0.06.
  • the complexing agent can be combined with an aqueous gel containing one or more hydrated polysaccharides and/or hydrated synthetic polymers having a pH in the range of from about 3 to about 12 at a temperature in the range of from about 40° F. to about 400° F. and preferably up to about 100° to 120° F.
  • the mixture is agitated and as the complexing agent dissolved it reacts with the hydrated polymers contained in the aqueous gel to form a highly viscous complexed aqueous gel.
  • the complexing agent is combined with the aqueous gel in an amount whereby the weight ratio of complexing agent to gelling agent contained in the aqueous gel is in the range of from about 0.01 to about 0.20, most preferably, in the range of from about 0.04 to about 0.08.
  • the additives are combined with an aqueous fluid having a pH in the range of from about 3 to about 12 and a temperature of from about 40° F. to about 400° F. and preferably up to about 100° to 120° F., while agitating the resultant mixture.
  • the solid hydratable gelling agent in the additive is dissolved in the aqueous fluid at a comparatively rapid rate whereby the gelling agent is hydrated followed by the dissolution of the complexing agent and the complexing reaction between the gelling agent and complexing agent.
  • the complexing agents and additives can be combined with the aqueous gel and aqueous fluid respectively in a static condition or they can be continuously combined while the resulting mixture is being pumped to a point of use, e.g., through a well bore and into a subterranean formation.
  • the solid additives are preferably combined with the aqueous fluid in an amount in the range of from about 0.25% by weight to about 1.5% by weight, most preferably in an amount in the range of from about 0.5% to about 1.0% by weight.
  • the high viscosity complexed aqueous gels of this invention are comprised of water, a gelling agent selected from the group consisting of hydratable polysaccharides, hydratable synthetic polymers and mixtures of such gelling agents present in the aqueous gel in an amount in the range of from about 0.2 to about 1.35% by weight thereof, and a complexing agent comprised of organic titanate monomers, homopolymers of such monomers and mixtures thereof, the monomers having the general formula:
  • R 1 is a bidentate organic ligand having one covalent bond and one coordinate covalent bond and having from 2 to 18 carbon atoms selected from the group consisting of ⁇ , ⁇ and ⁇ hydroxy acids, ⁇ , ⁇ and ⁇ hydroxy esters, ⁇ , ⁇ and ⁇ hydroxy aldehydes, ⁇ , ⁇ and ⁇ hydroxy ketones, ⁇ , ⁇ and ⁇ hydroxy ethers and ⁇ , ⁇ and ⁇ sulfur containing groups;
  • R 2 is a monodentate organic ligand having from 1 to 18 carbon atoms selected from the group consisting of alkoxy, aryloxy and other hydroxy organic groups
  • w is an integer in the range of from 1 to 4;
  • x is 0 or an integer in the range of from 1 to 3;
  • y is 0 or an integer in the range of from 1 to 3;
  • z is 0 or an integer in the range of from 1 to 3;
  • said complexing agent being present in said aqueous gel in an amount in the range of from about 0.01% to about 0.2% by weight.
  • the complexing agent in the above-described high viscosity complexed aqueous gel is comprised of organic titanate monomers, homopolymers of said monomers and mixtures thereof, the monomers having the general formula:
  • R 1 is a bidentate organic ligand having one covalent bond and one coordinate covalent bond and having 2 to 18 carbon atoms selected from the group consisting of ⁇ , ⁇ and ⁇ hydroxy acids, ⁇ , ⁇ and ⁇ hydroxy esters, ⁇ , ⁇ and ⁇ hydroxy aldehydes, ⁇ , ⁇ and ⁇ hydroxy ketones, ⁇ , ⁇ and ⁇ hydroxy ethers and ⁇ , ⁇ and ⁇ hydroxy sulfur containing groups;
  • w is an integer from 1 to 2;
  • y is 0-3;
  • z is 0-3.
  • the most preferred high viscosity complexed aqueous gel of this invention is comprised of water; hydroxypropylguar gelling agent present in said aqueous gel in the amount of 0.72% by weight of said aqueous gel and a complexing agent comprised of an organic titanate monomer, homopolymers of such monomer and mixtures thereof wherein the monomer is titanium bis acetylacetone-enolate dihydroxide and the complexing agent is present in said aqueous gel in an amount of 0.043% by weight.
  • the high viscosity complexed aqueous gels of this invention can include other components to bring about desired properties such as secondary gel, gel breakers, buffers, surfactants, fluid loss additives, solid materials such as sand or other proppants, etc.
  • the complexing agent of this invention is a solid crystalline material, has limited solubility in aqueous fluids and reacts with gelling agents of the type described herein over a broad pH and temperature range, it is particularly suitable for forming highly viscous aqueous treating fluid utilized in subterranean well formation treatments.
  • the powdered solid additives of this invention for forming the highly viscous complexed gels when combined with an aqueous fluid are particularly suitable for use in preparing highly viscous treating fluids for carrying out subterranean well formation treatments in that the gelling agent and complexing agent compounds of the additives as well as other desired components can be premixed in dry solid form, stored in suitable containers, transported to an area of use and combined directly with an aqueous fluid in a batch or continuous manner.
  • a complexing agent of this invention namely, a solid mixture of titanium bis acetylacetoneenolate dihydroxide monomer and homopolymers of such monomer
  • a solid gelling agent mixture comprised of 91% by weight hydroxypropylguar, 5.5% by weight fumaric acid and 3.5% by weight sodium bicarbonate in the proportions indicated in Table I below.
  • the resulting dry solid additives are combined with quantities of tap water in a Waring blender in the amounts indicated and at the temperatures given in Table I while mixing at a moderate speed.
  • Example 1 The procedure of Example 1 is repeated except that tap water containing 2% potassium chloride is used at a temperature in the range of from 70° F. to 75° F.
  • the pH of the complexed gels formed ranges from about 5 to about 7.
  • Example 2 The procedure described in Example 1 is repeated except that additives containing 50 parts by weight of the gelling agent mixture and 4 parts by weight complexing agent are added to tap water containing 2% potassium chloride at various concentrations.
  • the temperature of the water is in the range of from about 70° F. to about 75° F. and the pH of the resulting complexed gels ranges from about 5 to about 7.
  • Table III The results of these tests are shown in Table III below.
  • Example 3 The procedure described in Example 3 is repeated except that tap water containing 10% sodium chloride is utilized. The results of these tests are given in Table IV below.
  • Example 3 The procedure described in Example 3 is repeated except that the additives contain 50 parts by weight of the gelling agent mixture and 3 parts by weight complexing agent. The results of these tests are shown in Table V below.
  • Example 1 The procedure described in Example 1 is repeated except that additives are prepared containing various quantities of complexing agent and the temperature of the water used is 40° F. The results of these tests are shown in Table VI below.
  • a solid additive of the present invention is prepared by blending 45 parts by weight hydroxypropylguar gelling agent with 5 parts by weight complexing agent, namely, a solid mixture of titanium bis acetylacetone-enolate dihydroxide monomers and homopolymers.
  • Portions of tap water containing 1% potassium chloride are prepared at various pH levels by combining buffers therewith.
  • the buffers used are mixtures of fumaric acid, sodium bicarbonate and sodium hydroxide.
  • Portions of the additive are combined with the water in quantities of 50 pounds of additive per 1,000 gallons of water and the complex times are determined in accordance with the procedure given in Example 1. The results of these tests are given in Table VII below.
  • Example 1 The procedure described in Example 1 is repeated except that various water temperatures are utilized. The results of these tests are given in Table VIII below.
  • An additive of the present invention is prepared comprised of 60 parts by weight of a gelling agent containing 91% by weight hydroxypropylguar, 5.5% by weight fumaric acid and 3.5% by weight sodium bicarbonate and 6 parts by weight of the complexing agent described in Example 1.
  • the additive is combined with tap water containing 2% potassium chloride in the amount of 66 pounds per 1,000 gallons of water.
  • the apparent viscosity of the complexed aqueous gel produced is determined at various temperatures using a Model 50A FANN viscometer with modified bob at 300 rpm. The results of these tests are given in Table IX below.

Abstract

High viscosity complexed aqueous gels and methods and additives for forming such gels utilizing solid crystalline organic titanate complexing agents are provided. The organic titanate complexing agents react over broad pH and temperature ranges and the reaction rates thereof are controlled by the rate of dissolution of the agents.

Description

High viscosity aqueous gels containing hydrated organic polymers crosslinked or complexed by metal containing complexing agents have been developed heretofore. Such complex aqueous gels have a variety of uses including, but not limited to, suspending explosive materials used in mining, drilling and other similar applications, carrying out production stimulation procedures in oil, gas and water wells, carrying out subterranean well completions, transporting proppant or other materials into desired areas in subterranean well formations, diverting fluids in subterranean well formations, and carrying out cleaning procedures such as in cleaning of tubular goods, production equipment and industrial equipment.
High viscosity aqueous gels are particularly suitable as treating fluids in carrying out subterranean well formation acidizing, fracturing and fracture acidizing procedures. The high viscosity of the treating fluids prevents acid therein from becoming prematurely spent and inactive, enables the development of wider fractures in fracturing and fracture acidizing procedures, permits better fluid loss control and increases the proppant or other particulated material carrying capacity of the treating fluids.
Hydrophilic organic polymers (hereinafter referred to as gelling agents) such as hydratable polysaccharides and hydratable synthetic polymers, e.g., polyacrylamide, have been widely used to form aqueous gels. Numerous solid metallic crosslinking or complexing agents have also been employed to complex the hydrated gelling agents thereby forming a highly viscous aqueous fluid. The metallic complexing agents used heretofore include antimony salts, aluminum salts, chromium salts, and certain organic titanates. However, all of such complexing agents are limited in their use in that specific conditions of pH, temperature, other chemicals, etc. are required for the complexing reaction between the complexing agent and the hydrated organic polymers utilized to take place. For example, antimony complexing agents require that the aqueous gel have a specific pH and temperature before the complexing reaction takes place. Other metallic complexing agents such as chromium salts require oxidation-reduction for crosslinking. In addition, heretofore used complexing agents require separate mixing with the aqueous gel formed after the hydrated organic polymer or polymers utilized have been hydrated thereby requiring the use of elaborate mixing procedures and equipment for preparing the desired high viscosity complexed aqueous gels.
By the present invention a solid crystalline complexing agent is provided which reacts with aqueous gels containing hydrated organic polymers such as polysaccharides and polyacrylamides to form the aqueous gel into a high viscosity complexed aqueous fluid over a broad range of pH and temperature conditions. In addition, by the present invention solid additives are provided containing one or more hydratable organic polymers and the aforesaid complexing agent which can be combined directly with an aqueous fluid to form a highly viscous complexed aqueous gel at a desired pH and/or temperature. High viscosity complexed aqueous gels and methods of forming such gels utilizing the complexing agents and additives of this invention are also provided.
The complexing agents of this invention are solid crystalline materials comprised of organic titanate monomers, homopolymers of such monomers and mixtures of such monomers and homopolymers, the monomers having the following general formula:
Ti(--R.sub.1 --).sub.w (--R.sub.2 --).sub.x (--OH).sub.y (--O--).sub.z
wherein:
R1 is a bidentate organic ligand having one covalent bond and one coordinate covalent bond and having from 2 to 18 carbon atoms selected from the group consisting of α, β and γ hydroxy acids, α, β and γ hydroxy esters, α, β and γ hydroxy aldehydes, α, β and γ hydroxy ketones, α, β and γ hydroxy ethers, α, β and γ sulfur containing groups, and α, β and γ amines;
R2 is a monodentate organic ligand having from 1 to 18 carbon atoms selected from the group consisting of alkoxy, aryloxy and other hydroxy organic groups;
w is an integer in the range of from 1 to 4;
x is 0 or an integer in the range of from 1 to 3;
y is 0 or an integer in the range of from 1 to 3; and
z is 0 or an integer in the range of from 1 to 3.
Examples of R1 ligands which can be present in the organic titanate monomer are 2,2',2" nitrilodiethanol monoethoxide, acetylacetone-enolate and ammonium propanate-2-oxide. Examples of R2 groups which can be present in the monomer are methoxy, ethoxy, propoxy, isopropoxy, butoxy, phenoxy and octadecoxy. Of these, methoxy, butoxy and isopropoxy are preferred with isopropoxy being the most preferred.
A more preferred complexing agent of the present invention is a solid crystalline material comprised of organic titanate monomers, homopolymers of such monomers and mixtures of such monomers and homopolymers, the monomers having the general formula:
Ti(--R.sub.1 --).sub.w (--OH).sub.y (--O--).sub.z
wherein:
R1 is a group of the type described above; w is an integer of from 1 to 2; y is 0 to 3; and z is 0 to 3. Examples of such monomers are titanium bis [2,2',2" nitrilodiethanol monoethoxide] dihydroxide, titanium bis acetylacetone-enolate dihydroxide, and titanium bis [ ammonium propanate-2-oxide] dihydroxide. Of these, titanium bis acetylacetone-enolate dihydroxide is the most preferred.
The most preferred complexing agent of the present invention is comprised of an organic titanate monomer, homopolymers of such monomer and mixtures thereof wherein said monomer is titanium bis acetylacetone-enolate dihydroxide.
The solid crystalline complexing agents of this invention can be prepared in various ways. For example, a tetra-alkoxy titanate can be reacted with an organic ketone, ester, amine or alcohol to produce a reaction product which when hydrolyzed forms the solid crystalline organic titanate complexing agent of this invention. For example, titanium (IV) tetraisopropoxide can be reacted with acetylacetone in a 1:2 mole ratio to form titanium bis acetylacetone-enolate bis isopropoxide. This reaction product can then be combined with excess water at room temperature with moderate agitation to yield the organic titanate complexing agent of this invention as a precipitate. When dried, the precipitate is a white to yellow powder, crystalline in nature.
An alternate procedure which can be utilized to form the organic titanate complexing agents of this invention is to react a titanium tetrahalide with an organic acetone, acetate, amine or alcohol in the presence of water and a base. For example, titanium tetrachloride can be reacted with acetylacetone in a 1:1 mole ratio in excess water and a base for neutralization to form the solid organic titanate.
As indicated above, the complexing agents of this invention react with hydrated gelling agents to complex such gelling agents and form a highly viscous complexed aqueous gel over a broad pH and temperature range, i.e., at a pH in the range of from about 3 to about 12 and at a temperature in the range of from about 40° F. to about 400° F., and preferably up to about 100° to 120° F. Solid hydratable gelling agents which are preferred for use in accordance with this invention are hydratable polysaccharides and hydratable synthetic polymers such as polyacrylamides. Particularly preferred hydratable polysaccharides are gelactomannan gums and derivatives thereof, glucomannan gums and derivatives thereof, and cellulose derivatives. Examples of such compounds are guar gum, locust bean gum, karaya gum, sodium carboxymethylguar, hydroxyethylguar, sodium carboxymethylhydroxyethylguar, hydroxypropylguar, sodium carboxymethylhydroxypropylcellulose, sodium carboxyethylhydroxyethylcellulose, and hydroxyethylcellulose. The hydroxyethylcellulose derivative used as gelling agents should be those having between 0.5 and about 10 moles of ethylene oxide per anhydroglucose unit. The most preferred gelling agent for use in accordance with this invention is hydroxypropylguar.
Because the complexing agent of this invention is a crystalline material of fine particle size, it can be uniformly mixed with one or more of the solid gelling agents described above to form a solid powder additive which can be combined directly with an aqueous fluid, either in a batch or continuous process, to form a highly viscous complexed aqueous gel. The organic titanate complexing agent is dissolved in aqueous fluids at a slower rate than the gelling agents described above thereby allowing the gelling agents to hydrate prior to being complexed by the complexing agent when the gelling agent and complexing agent are added to an aqueous fluid simultaneously. In addition to the organic titanate complexing agent and one or more gelling agents of the type described above, the additives of this invention for forming high viscosity complexed aqueous gels can include a variety of other solid chemicals to bring about desired results. For example, breakers for the complexed gels produced by the additives can be included in the additives such as oxidizing agents, enzymes, acids and mixtures of such compounds. Examples of particularly suitable oxidizing agents are sodium persulfate and ammonium persulfate. Examples of suitable enzymes which can be used are α and β amylases, amyloglucosidase, aligoglucosidase, invertase, maltase, cellulase and hemicellulase. An example of a suitable acid is fumaric acid. Of these, a mixture of sodium persulfate, hemicellulase and cellulase is perferred. Other solid additives such as buffers, surface active agents, fluid loss control chemicals, etc., can also be included.
A preferred solid additive for forming the high viscosity complexed aqueous gels of this invention when combined with an aqueous fluid is comprised of a mixture of a gelling agent selected from the group consisting of solid hydratable polysaccharides, hydratable synthetic polymers and mixtures thereof, and a solid complexing agent comprised of organic titanate monomers, homopolymers of such monomers and mixtures thereof, the monomers having the following general formula:
Ti(--R.sub.1 --).sub.w (--R.sub.2 --).sub.x (--OH).sub.y (--O--).sub.z
wherein:
R1 is a bidentate organic ligand having one covalent bond and one coordinate covalent bond and having from 2 to 18 carbon atoms selected from the group consisting of α, β and γ hydroxy acids, α, β and γ hydroxy ketones, α, β and γ hydroxy ethers and α, β and γ hydroxy sulfur containing groups;
R2 is a monodentate organic ligand having from 1 to 18 carbon atoms selected from the group consisting of alkoxy, aryloxy and other hydroxy organic groups;
w is an integer in the range of from 1 to 4;
x is 0 or an integer in the range of from 1 to 3;
y is 0 or an integer in the range of from 1 to 3; and
z is 0 or an integer in the range of from 1 to 3.
A more preferred additive of this invention is comprised of a mixture of a solid gelling agent selected from the group consisting of sodium carboxymethylhydroxyethylcellulose, guar, hydroxypropylguar, hydratable polyacrylamide and mixtures thereof, and a solid complexing agent comprised of organic titanate monomers, homopolymers and mixtures of such monomers and homopolymers, the monomers having the following general formula:
Ti(--R.sub.1 --).sub.w (--OH).sub.y (--O--).sub.z
wherein:
R1 is a bidentate organic ligand having one covalent bond and one coordinate covalent bond and having from 2 to 18 carbon atoms selected from the group consisting of α, β and γ hydroxy acids, α, β and γ hydroxy esters, α, β and γ hydroxy aldehydes, α, β and γ hydroxy ketones and α, β and γ hydroxy ethers, and α, β and γ hydroxy sulfur containing groups;
w is an integer from 1 to 2;
y is 0 to 3; and
z is 0 to 3.
The most preferred additive of this invention comprises a mixture of solid hydroxypropylguar gelling agent and a solid complexing agent comprised of an organic titanate monomer, homopolymers of such monomer and mixtures thereof wherein said monomer is titanium bis acetylacetone-enolate dihydroxide.
The solid additives of this invention for forming highly viscous complexed aqueous gels when combined with an aqueous fluid preferably include complexing agent and gelling agent in amounts whereby the weight ratio of complexing agent to gelling agent is in the range of from about 0.01 to about 0.20. A more preferred additive contains complexing agent to gelling agent in a weight ratio in the range of from about 0.02 to about 0.10, and the most preferred additive contains complexing agent to gelling agent in a weight ratio of 0.06.
In forming a high viscosity complexed aqueous gel using the complexing agents of this invention, the complexing agent can be combined with an aqueous gel containing one or more hydrated polysaccharides and/or hydrated synthetic polymers having a pH in the range of from about 3 to about 12 at a temperature in the range of from about 40° F. to about 400° F. and preferably up to about 100° to 120° F. The mixture is agitated and as the complexing agent dissolved it reacts with the hydrated polymers contained in the aqueous gel to form a highly viscous complexed aqueous gel. Preferably, the complexing agent is combined with the aqueous gel in an amount whereby the weight ratio of complexing agent to gelling agent contained in the aqueous gel is in the range of from about 0.01 to about 0.20, most preferably, in the range of from about 0.04 to about 0.08.
In forming a complexed aqueous gel using the solid additives of the present invention, the additives are combined with an aqueous fluid having a pH in the range of from about 3 to about 12 and a temperature of from about 40° F. to about 400° F. and preferably up to about 100° to 120° F., while agitating the resultant mixture. The solid hydratable gelling agent in the additive is dissolved in the aqueous fluid at a comparatively rapid rate whereby the gelling agent is hydrated followed by the dissolution of the complexing agent and the complexing reaction between the gelling agent and complexing agent. As indicated above, the complexing agents and additives can be combined with the aqueous gel and aqueous fluid respectively in a static condition or they can be continuously combined while the resulting mixture is being pumped to a point of use, e.g., through a well bore and into a subterranean formation. The solid additives are preferably combined with the aqueous fluid in an amount in the range of from about 0.25% by weight to about 1.5% by weight, most preferably in an amount in the range of from about 0.5% to about 1.0% by weight.
The high viscosity complexed aqueous gels of this invention are comprised of water, a gelling agent selected from the group consisting of hydratable polysaccharides, hydratable synthetic polymers and mixtures of such gelling agents present in the aqueous gel in an amount in the range of from about 0.2 to about 1.35% by weight thereof, and a complexing agent comprised of organic titanate monomers, homopolymers of such monomers and mixtures thereof, the monomers having the general formula:
Ti(--R.sub.1 --).sub.w (--R.sub.2 --).sub.x (--OH).sub.y (--O--).sub.z
wherein:
R1 is a bidentate organic ligand having one covalent bond and one coordinate covalent bond and having from 2 to 18 carbon atoms selected from the group consisting of α, β and γ hydroxy acids, α, β and γ hydroxy esters, α, β and γ hydroxy aldehydes, α, β and γ hydroxy ketones, α, β and γ hydroxy ethers and α, β and γ sulfur containing groups;
R2 is a monodentate organic ligand having from 1 to 18 carbon atoms selected from the group consisting of alkoxy, aryloxy and other hydroxy organic groups
w is an integer in the range of from 1 to 4;
x is 0 or an integer in the range of from 1 to 3;
y is 0 or an integer in the range of from 1 to 3; and
z is 0 or an integer in the range of from 1 to 3;
said complexing agent being present in said aqueous gel in an amount in the range of from about 0.01% to about 0.2% by weight.
More preferably, the complexing agent in the above-described high viscosity complexed aqueous gel is comprised of organic titanate monomers, homopolymers of said monomers and mixtures thereof, the monomers having the general formula:
Ti(--R.sub.1 --).sub.w (--OH).sub.y (--O--).sub.z
wherein:
R1 is a bidentate organic ligand having one covalent bond and one coordinate covalent bond and having 2 to 18 carbon atoms selected from the group consisting of α, β and γ hydroxy acids, α, β and γ hydroxy esters, α, β and γ hydroxy aldehydes, α, β and γ hydroxy ketones, α, β and γ hydroxy ethers and α, β and γ hydroxy sulfur containing groups;
w is an integer from 1 to 2;
y is 0-3; and
z is 0-3.
The most preferred high viscosity complexed aqueous gel of this invention is comprised of water; hydroxypropylguar gelling agent present in said aqueous gel in the amount of 0.72% by weight of said aqueous gel and a complexing agent comprised of an organic titanate monomer, homopolymers of such monomer and mixtures thereof wherein the monomer is titanium bis acetylacetone-enolate dihydroxide and the complexing agent is present in said aqueous gel in an amount of 0.043% by weight.
As will be understood by those skilled in the art, the high viscosity complexed aqueous gels of this invention can include other components to bring about desired properties such as secondary gel, gel breakers, buffers, surfactants, fluid loss additives, solid materials such as sand or other proppants, etc. As indicated above, because the complexing agent of this invention is a solid crystalline material, has limited solubility in aqueous fluids and reacts with gelling agents of the type described herein over a broad pH and temperature range, it is particularly suitable for forming highly viscous aqueous treating fluid utilized in subterranean well formation treatments. Further, the powdered solid additives of this invention for forming the highly viscous complexed gels when combined with an aqueous fluid are particularly suitable for use in preparing highly viscous treating fluids for carrying out subterranean well formation treatments in that the gelling agent and complexing agent compounds of the additives as well as other desired components can be premixed in dry solid form, stored in suitable containers, transported to an area of use and combined directly with an aqueous fluid in a batch or continuous manner.
In order to more clearly illustrate the present invention, the following examples are given.
EXAMPLE 1
In the laboratory, quatities of a complexing agent of this invention, namely, a solid mixture of titanium bis acetylacetoneenolate dihydroxide monomer and homopolymers of such monomer, are combined with a solid gelling agent mixture comprised of 91% by weight hydroxypropylguar, 5.5% by weight fumaric acid and 3.5% by weight sodium bicarbonate in the proportions indicated in Table I below. The resulting dry solid additives are combined with quantities of tap water in a Waring blender in the amounts indicated and at the temperatures given in Table I while mixing at a moderate speed. Each of the tests are conducted using the same Waring blender mixing speed, and the time required for the vortex produced by the blender to close and the gel produced therein to roll in the blender is recorded as the time required for a complexed gel to form. The pH of the gels produced is also determined. The results of these tests are given in Table I below.
                                  TABLE I                                 
__________________________________________________________________________
COMPLEXED AQUEOUS GEL FORMATION USING SOLID GELLING AGENT -               
COMPLEXING AGENT ADDITIVES                                                
                 QUANTITY OF GEL-                                         
                 LING AGENT AND                                           
QUANTITY OF COMPLEXING                                                    
                 OTHER ADDITIVES                                          
                              WATER                                       
                                   COMPLEX                                
AGENT, LBS/1000  USED, LBS/1000                                           
                              TEMP.,                                      
                                   TIME,  GEL                             
GALLONS OF WATER GALLONS OF WATER                                         
                              °F.                                  
                                   SECONDS                                
                                          pH                              
__________________________________________________________________________
5                50           60   405    5.07                            
5                50           100  180    5.28                            
3                50           60   540    5.11                            
__________________________________________________________________________
EXAMPLE 2
The procedure of Example 1 is repeated except that tap water containing 2% potassium chloride is used at a temperature in the range of from 70° F. to 75° F. The pH of the complexed gels formed ranges from about 5 to about 7.
                                  TABLE II                                
__________________________________________________________________________
COMPLEXED AQUEOUS GELL FORMATION AT VARIOUS                               
COMPLEXING AGENT CONCENTRATIONS                                           
               QUANTITY OF GEL-                                           
               LING AGENT AND                                             
QUANTITY OF COMPLEX-                                                      
               OTHER ADDITIVES                                            
                            COMPLEX                                       
ING AGENT, LBS/1000                                                       
               USED, LBS/1000                                             
                            TIME,  OBSERVATIONS OF                        
GALLONS OF WATER                                                          
               GALLONS OF WATER                                           
                            SECONDS                                       
                                   COMPLEXED GEL                          
__________________________________________________________________________
5              50           125    CHUNKY COMPLEX                         
4              50           135    GOOD COMPLEX                           
3              50           140    GOOD COMPLEX                           
2              50           205    GOOD COMPLEX                           
1              50           480    GOOD COMPLEX                           
__________________________________________________________________________
From Table II it can be seen that good complexes are rapidly formed at complexing agent concentrations of from about 2 to about 4 lbs. per 1,000 gallons of water and gelling agent concentrations of 50 lbs. per 1,000 gallons of water.
EXAMPLE 3
The procedure described in Example 1 is repeated except that additives containing 50 parts by weight of the gelling agent mixture and 4 parts by weight complexing agent are added to tap water containing 2% potassium chloride at various concentrations. The temperature of the water is in the range of from about 70° F. to about 75° F. and the pH of the resulting complexed gels ranges from about 5 to about 7. The results of these tests are shown in Table III below.
              TABLE III                                                   
______________________________________                                    
COMPLEXED AQUEOUS GEL FORMATION                                           
AT VARIOUS CONCENTRATIONS OF                                              
GELLING AGENT - COMPLEXING AGENT ADDITIVE                                 
QUANTITY OF GELLING                                                       
AGENT - COMPLEXING                                                        
                 COM-                                                     
AGENT ADDITIVE,  PLEX      OBSERVATIONS                                   
LBS/1000 GALLONS TIME,     OF COMPLEXED                                   
OF WATER         SECONDS   GEL                                            
______________________________________                                    
80               145       GOOD COMPLEX                                   
60               175       GOOD COMPLEX                                   
50               180       GOOD COMPLEX                                   
40               240       WEAK COMPLEX                                   
30               300       WEAK COMPLEX                                   
20               300       WEAK COMPLEX                                   
______________________________________                                    
From Table III it can be seen that good complexes are rapidly formed at additive concentrations of from about 50 to about 80 lbs. of additive per 1,000 gallons of water used.
EXAMPLE 4
The procedure described in Example 3 is repeated except that tap water containing 10% sodium chloride is utilized. The results of these tests are given in Table IV below.
              TABLE IV                                                    
______________________________________                                    
COMPLEXED AQUEOUS GEL FORMATION AT VARIOUS                                
CONCENTRATIONS OF GELLING AGENT -                                         
COMPLEXING AGENT ADDITIVE IN WATER                                        
CONTAINING 10% BY WEIGHT NaCl                                             
QUANTITY OF GELLING                                                       
AGENT - COMPLEXING                                                        
                 COM-                                                     
AGENT ADDITIVE,  PLEX      OBSERVATIONS                                   
LBS/1000 GALLONS TIME,     OF COMPLEXED                                   
OF WATER         SECONDS   GEL                                            
______________________________________                                    
80               105       GOOD COMPLEX                                   
60               130       GOOD COMPLEX                                   
50               150       GOOD COMPLEX                                   
40               240       WEAK COMPLEX                                   
30               240       WEAK COMPLEX                                   
20               270       WEAK COMPLEX                                   
______________________________________                                    
From Table IV it can be seen that good complexes are rapidly formed in salt water at additive concentrations of from about 50 to about 80 lbs. per 1,000 gallons of water used.
EXAMPLE 5
The procedure described in Example 3 is repeated except that the additives contain 50 parts by weight of the gelling agent mixture and 3 parts by weight complexing agent. The results of these tests are shown in Table V below.
              TABLE V                                                     
______________________________________                                    
COMPLEXED AQUEOUS GEL FORMATION AT VARIOUS                                
CONCENTRATIONS OF GELLING AGENT -                                         
COMPLEXING AGENT ADDITIVE IN WATER                                        
QUANTITY OF GELLING                                                       
AGENT - COMPLEXING                                                        
                 COM-                                                     
AGENT ADDITIVE,  PLEX      OBSERVATIONS                                   
LBS/1000 GALLONS TIME,     OF COMPLEXED                                   
OF WATER         SECONDS   GEL                                            
______________________________________                                    
80               210       GOOD COMPLEX                                   
60               220       GOOD COMPLEX                                   
50               200       GOOD COMPLEX                                   
40               240       WEAK COMPLEX                                   
30               240       WEAK COMPLEX                                   
20               270       WEAK COMPLEX                                   
______________________________________                                    
From Table V it can be seen that good complexes are rapidly formed at additive concentrations of from about 50 to about 80 lbs. per 1,000 gallons of water. From a comparison of Tables IV and V it can be seen that 50 parts by weight gelling agent and 4 parts by weight complexing agent form good complexes more rapidly than those containing 50 parts by weight gelling agent and 3 parts by weight complexing agent.
EXAMPLE 6
The procedure described in Example 1 is repeated except that additives are prepared containing various quantities of complexing agent and the temperature of the water used is 40° F. The results of these tests are shown in Table VI below.
                                  TABLE VI                                
__________________________________________________________________________
COMPLEXED AQUEOUS GEL FORMATION AT VARIOUS CONCENTRATIONS OF              
COMPLEXING AGENT IN WATER AT 40° F.                                
QUANTITY OF COMPLEXING                                                    
                 QUANTITY OF GELLING AGENT                                
                                    COMPLEX                               
AGENT, LBS/1000 GALLONS                                                   
                 AND OTHER ADDITIVES USED,                                
                                    TIME,                                 
OF WATER         LB/1000 GALLONS OF WATER                                 
                                    SECONDS                               
__________________________________________________________________________
5                50                 750                                   
4                50                 750                                   
3                50                 750                                   
__________________________________________________________________________
From Table VI it can be seen that the additives of this invention are effective in forming complexed aqueous gels at water temperatures of 40° F.
EXAMPLE 7
A solid additive of the present invention is prepared by blending 45 parts by weight hydroxypropylguar gelling agent with 5 parts by weight complexing agent, namely, a solid mixture of titanium bis acetylacetone-enolate dihydroxide monomers and homopolymers. Portions of tap water containing 1% potassium chloride are prepared at various pH levels by combining buffers therewith. The buffers used are mixtures of fumaric acid, sodium bicarbonate and sodium hydroxide. Portions of the additive are combined with the water in quantities of 50 pounds of additive per 1,000 gallons of water and the complex times are determined in accordance with the procedure given in Example 1. The results of these tests are given in Table VII below.
              TABLE VII                                                   
______________________________________                                    
COMPLEXED AQUEOUS GEL FORMATION                                           
AT VARIOUS pH LEVELS                                                      
pH OF  COMPLEX TIME,                                                      
WATER  SECONDS         COMMENTS                                           
______________________________________                                    
3.3    150                                                                
4.1    135                                                                
4.5    135                                                                
7.1    --              GEL NOT FORMED.sup.1                               
7.6    --              GEL NOT FORMED.sup.1                               
9.14   --              GEL NOT FORMED.sup.1                               
7.6    12              GELLING AGENT                                      
                       PREHYDRATED                                        
8.2    8               GELLING AGENT                                      
                       PREHYDRATED                                        
9.3    9               GELLING AGENT                                      
                       PREHYDRATED                                        
______________________________________                                    
 .sup.1 Gelling agent will not hydrate in higher pH water.                
From Table VII it can be seen that the complexed aqueous gels of this invention can be formed using water at various pH levels.
EXAMPLE 8
The procedure described in Example 1 is repeated except that various water temperatures are utilized. The results of these tests are given in Table VIII below.
                                  TABLE VIII                              
__________________________________________________________________________
COMPLEXED AQUEOUS GEL FORMATION AT VARIOUS TEMPERATURES                   
QUANTITY OF COMPLEX-                                                      
               QUANTITY OF GELLING                                        
ING AGENT, LBS/1000                                                       
               AGENT, LBS/1000                                            
                              COMPLEX TIME,                               
                                        WATER TEMPERATURE,                
GALLONS OF WATER                                                          
               GALLONS OF WATER                                           
                              SECONDS   °F.                        
__________________________________________________________________________
5              50             120       72                                
5              50             150       40                                
5              50             50        110                               
__________________________________________________________________________
From Table VIII it can be seen that the complexed aqueous gels of this invention can be formed over a broad temperature range.
EXAMPLE 9
An additive of the present invention is prepared comprised of 60 parts by weight of a gelling agent containing 91% by weight hydroxypropylguar, 5.5% by weight fumaric acid and 3.5% by weight sodium bicarbonate and 6 parts by weight of the complexing agent described in Example 1. The additive is combined with tap water containing 2% potassium chloride in the amount of 66 pounds per 1,000 gallons of water. The apparent viscosity of the complexed aqueous gel produced is determined at various temperatures using a Model 50A FANN viscometer with modified bob at 300 rpm. The results of these tests are given in Table IX below.
              TABLE IX                                                    
______________________________________                                    
VISCOSITY OF COMPLEXED AQUEOUS GEL                                        
TEMPERATURE,                                                              
°F.      VISCOSITY.sup.1, CP                                       
______________________________________                                    
80              1000                                                      
100             1100                                                      
125             1100                                                      
150             1000                                                      
175             900                                                       
200             750                                                       
225             600                                                       
250             450                                                       
275             250                                                       
300             200                                                       
325             200                                                       
350             110                                                       
375             40                                                        
400             30                                                        
______________________________________                                    
 .sup.1 Measured on a Model 50A FANN viscometer, 300 rpm, 400 psig.       
 modified bob.                                                            
From Table IX it can be seen that the complexed aqueous gels of this invention are stable over a broad temperature range.

Claims (9)

What is claimed is:
1. A solid additive for forming a high viscosity complexed aqueous gel when combined with water comprising:
a solid gelling agent selected from the group consisting of hydratable polysaccharides and hydratable synthetic polymers; and
a complexing agent selected from the group consisting organic titanate monomers, homopolymers of such monomers and mixtures thereof present in said solid additive in an amount whereby the weight ratio of complexing agent to gelling agent is in the range of from about 0.01 to about 0.2, the monomers having the general formula:
Ti(--R.sub.1 --).sub.w (--R.sub.2 --).sub.x (--OH).sub.y (--O--).sub.z
wherein:
R1 is a bidentate organic ligand having one covalent bond and one one coordinate covalent bond and having from 2 to 18 carbon atoms selected from the group consisting of α, β and γ hydroxy acids, α, β and γ hydroxy esters, α, β and γ hydroxy aldehydes, α, β and γ hydroxy ketones, α, β and γ hydroxy ethers, α, β and γ sulfur containing groups, and α, β and γ amines;
R2 is a monodentate organic ligand having from 1 to 18 carbon atoms selected from the group consisting of alkoxy, aryloxy and other hydroxy organic groups;
w is an integer in the range of from 1 to 4;
x is 0 or an integer in the range of from 1 to 3;
y is 0 or an integer in the range of from 1 to 3; and
z is 0 or an integer in the range of from 1 to 3.
2. The additive of claim 1 wherein said gelling agent is selected from the group consisting of guar, carboxymethylhydroxyethylcellulose, hydroxypropylguar and polyacrylamide, and said complexing agent is comprised of organic titanate monomers, homopolymers of said monomers and mixtures thereof, the monomers having the general formula:
Ti(--R.sub.1 --).sub.w (--OH).sub.y (--O--).sub.z
wherein:
R1 is a bidentate organic ligand having one covalent bond and one coordinate covalent bond and having from 1 to 18 carbon atoms selected from the group consisting of α, β and γ hydroxy acids, α, β and γ hydroxy esters, α, β and γ hydroxy aldehydes, α, β and γ hydroxy ketones, α, β and γ hydroxy ethers, α, β and γ sulfur containing groups, and α, β and γ amines;
w is an integer from 1 to 3;
y is 0 to 3; and
z is 0 to 3.
3. The solid additive of claim 1 wherein said organic titanate monomers are selected from the group consisting of titanium bis [2,2',2" nitrilodiethanol monoethoxide] dihydroxide, titanium bis acetylacetone-enolate dihydroxide and titanium bis dihydroxide.
4. The solid additive of claim 1 wherein said organic titanate monomer is titanium bis acetylacetone-enolate dihydroxide.
5. The additive of claim 1 wherein said gelling agent is hydroxypropylguar and said complexing agent is a solid mixture of titanium bis acetylacetone-enolate dihydroxide monomer and homopolymers of such monomer, and said gelling agent and complexing agent are present in said additive in amounts whereby the weight ratio of complexing agent to gelling agent is 0.06.
6. A method of forming a high viscosity complexed aqueous gel comprising the steps of:
combining an additive with water to form said complexed aqueous gelled fluid, said additive being comprised of:
a solid gelling agent selected from the group consisting of hydratable polysaccharides and hydratable synthetic polymers; and
a complexing agent selected from the group consisting of organic titanate monomers, homopolymers of such monomers and mixtures thereof present in said additive in an amount whereby the weight ratio of complexing agent to gelling agent in said additive is in the range of from about 0.01 to about 0.2, the monomers having the general formula:
Ti(--R.sub.1 --).sub.w (--R.sub.2 --).sub.x (--OH).sub.y (--O--).sub.z
wherein:
R1 is a bidentate organic ligand having one covalent bond and one one coordinate covalent bond and having from 2 to 18 carbon atoms selected from the group consisting of α, β and γ hydroxy acids, α, β and γ hydroxy esters, α, β and γ hydroxy aldehydes, α, β and γ hydroxy ketones, α, β and γ hydroxy ethers, α, β and γ sulfur containing groups, and α, β and γ amines;
R2 is a monodentate organic ligand having from 1 to 18 carbon atoms selected from the group consisting of alkoxy, aryloxy and other hydroxy organic groups;
w is an integer in the range of from 1 to 4;
x is 0 or an integer in the range of from 1 to 3;
y is 0 or an integer in the range of from 1 to 3; and
z is 0 or an integer in the range of from 1 to 3.
7. The method of claim 6 wherein said gelling agent is selected from the group consisting of guar, carboxymethylhydroxyethylcellulose, hydroxypropylguar and polyacrylamide, and said complexing agent is comprised of organic titanate monomers, homopolymers of said monomers and mixtures thereof, the monomers having the general formula:
Ti(--R.sub.1 --).sub.w (--OH).sub.y (--O--).sub.z
wherein:
R1 is a bidentate organic ligand having one covalent bond and one coordinate covalent bond and having from 2 to 18 carbon atoms selected from the group consisting of α, β and γ hydroxy acids, α, β and γ hydroxy esters, α, β and γ hydroxy aldehydes, α, β and γ hydroxy ketones, α, β and γ hydroxy ethers, α, β and γ sulfur containing groups, and α, β and γ amines;
w is an integer from 1 to 2;
y is 0 to 3; and
z is 0 to 3.
8. The method of claim 6 wherein said gelling agent is hydroxypropylguar and said complexing agent is a mixture of titanium bis acetylacetone-enolate dihydroxide monomers and homopolymers of said monomers.
9. The method of claim 6 wherein said gelling agent is hydroxypropylguar and said complexing agent is a solid mixture of titanium bis acetylacetone-enolate dihydroxide monomer and homopolymers of such monomer, and said gelling agent and complexing agent are present in said additive in amounts whereby the weight ratio of complexing agent to gelling agent is 0.06.
US06/075,481 1979-09-14 1979-09-14 High viscosity complexed aqueous gels and methods and additives for forming such gels Expired - Lifetime US4369124A (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
US06/075,481 US4369124A (en) 1979-09-14 1979-09-14 High viscosity complexed aqueous gels and methods and additives for forming such gels
CA000351651A CA1140120A (en) 1979-09-14 1980-05-09 High viscosity complexed aqueous gels and methods and additives for forming such gels
AU58792/80A AU5879280A (en) 1979-09-14 1980-05-27 Organic titanate cross-linking agent
GB8018337A GB2058750A (en) 1979-09-14 1980-06-04 High viscosity complexed aqueous gels comprising organic titanite complexing agents
NO801679A NO801679L (en) 1979-09-14 1980-06-05 COMPLEX AQUEOUS GELLS WITH HIGH VISCOSITY, AND PROCEDURES AND ADDITIVES FOR THE PREPARATION OF SUCH GELS
NL8003501A NL8003501A (en) 1979-09-14 1980-06-17 HIGH VISCOSITY COMPLEX AQUEOUS GELS, METHODS AND ADDITIVES, FOR PREPARING SUCH GELS.
BR8004199A BR8004199A (en) 1979-09-14 1980-07-07 SOLID COMPLEXING AGENT, SOLID ADDITIVE, HIGH VISCOSITY AQUEOUS GEL, COMPLEX PROCESS AND INCREASING THE VISCOSITY OF A HIGH VISCOSITY GEL WASTE FLUID
IT24638/80A IT1141046B (en) 1979-09-14 1980-09-12 HIGH VISCOSITY COMPLEX AQUOUS GEL AND PROCEDURES AND ADDITIVES FOR PREPARING SUCH GEL
DE19803034721 DE3034721A1 (en) 1979-09-14 1980-09-15 COMPLEX AQUEOUS GELS WITH HIGH VISCOSITY, ADDITIVES AND METHOD FOR PRODUCING SUCH GELS

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US4505826A (en) * 1982-10-25 1985-03-19 Smith International Inc. Prepackaged crosslinked polymer
US4619776A (en) * 1985-07-02 1986-10-28 Texas United Chemical Corp. Crosslinked fracturing fluids
WO1987000236A1 (en) * 1985-07-02 1987-01-15 Texas United Chemical Corporation Crosslinked fracturing fluids
US4640358A (en) * 1984-03-26 1987-02-03 Mobil Oil Corporation Oil recovery process employing a complexed polysaccharide
US4647312A (en) * 1984-03-26 1987-03-03 Mobil Oil Corporation Oil recovery process employing a complexed polysaccharide
US4695389A (en) * 1984-03-16 1987-09-22 Dowell Schlumberger Incorporated Aqueous gelling and/or foaming agents for aqueous acids and methods of using the same
US4770796A (en) * 1987-01-12 1988-09-13 Petrolite Corporation Encapsulated breaker for cross-linked acid gel, fracture acidizing fluid containing same and method of use thereof
US4784694A (en) * 1982-12-21 1988-11-15 Etudes Et Fabrication Compositions of polymer systems, and their use for example in hydraulic fracturing
US5021171A (en) * 1989-03-20 1991-06-04 E. I. Du Pont De Nemours And Company Organotitanium compositions useful for cross-linking
US5271943A (en) * 1989-10-27 1993-12-21 Scott Health Care Wound gel compositions containing sodium chloride and method of using them
US5591699A (en) * 1993-02-24 1997-01-07 E. I. Du Pont De Nemours And Company Particle transport fluids thickened with acetylate free xanthan heteropolysaccharide biopolymer plus guar gum
US5827803A (en) * 1997-05-07 1998-10-27 Loree; Dwight N. Well treatment fluid
US20030196809A1 (en) * 2002-04-23 2003-10-23 Dean Willberg Method for preparing improved high temperature fracturing fluids
US20070060482A1 (en) * 2005-09-13 2007-03-15 Halliburton Energy Services, Inc. Methods and compositions for controlling the viscosity of viscoelastic surfactant fluids
US20070056736A1 (en) * 2005-09-13 2007-03-15 Halliburton Energy Services, Inc. Methods and compositions for controlling the viscosity of viscoelastic surfactant fluids

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DE3421443C2 (en) * 1984-06-08 1996-09-05 Daicel Chem Stable gel mass and process for its preparation
CA1262896A (en) * 1985-06-11 1989-11-14 Michael E. Morgan Titanium-glycol useful as crosslinking agents for polygalactomannans
US5412016A (en) * 1992-09-28 1995-05-02 E. I. Du Pont De Nemours And Company Process for making polymeric inorganic-organic compositions

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Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4505826A (en) * 1982-10-25 1985-03-19 Smith International Inc. Prepackaged crosslinked polymer
US4784694A (en) * 1982-12-21 1988-11-15 Etudes Et Fabrication Compositions of polymer systems, and their use for example in hydraulic fracturing
US4695389A (en) * 1984-03-16 1987-09-22 Dowell Schlumberger Incorporated Aqueous gelling and/or foaming agents for aqueous acids and methods of using the same
US4640358A (en) * 1984-03-26 1987-02-03 Mobil Oil Corporation Oil recovery process employing a complexed polysaccharide
US4647312A (en) * 1984-03-26 1987-03-03 Mobil Oil Corporation Oil recovery process employing a complexed polysaccharide
US4619776A (en) * 1985-07-02 1986-10-28 Texas United Chemical Corp. Crosslinked fracturing fluids
WO1987000236A1 (en) * 1985-07-02 1987-01-15 Texas United Chemical Corporation Crosslinked fracturing fluids
US4770796A (en) * 1987-01-12 1988-09-13 Petrolite Corporation Encapsulated breaker for cross-linked acid gel, fracture acidizing fluid containing same and method of use thereof
US5021171A (en) * 1989-03-20 1991-06-04 E. I. Du Pont De Nemours And Company Organotitanium compositions useful for cross-linking
US5271943A (en) * 1989-10-27 1993-12-21 Scott Health Care Wound gel compositions containing sodium chloride and method of using them
US5591699A (en) * 1993-02-24 1997-01-07 E. I. Du Pont De Nemours And Company Particle transport fluids thickened with acetylate free xanthan heteropolysaccharide biopolymer plus guar gum
US5827803A (en) * 1997-05-07 1998-10-27 Loree; Dwight N. Well treatment fluid
US20030196809A1 (en) * 2002-04-23 2003-10-23 Dean Willberg Method for preparing improved high temperature fracturing fluids
US6820694B2 (en) 2002-04-23 2004-11-23 Schlumberger Technology Corporation Method for preparing improved high temperature fracturing fluids
US20070060482A1 (en) * 2005-09-13 2007-03-15 Halliburton Energy Services, Inc. Methods and compositions for controlling the viscosity of viscoelastic surfactant fluids
US20070056736A1 (en) * 2005-09-13 2007-03-15 Halliburton Energy Services, Inc. Methods and compositions for controlling the viscosity of viscoelastic surfactant fluids
US7261160B2 (en) 2005-09-13 2007-08-28 Halliburton Energy Services, Inc. Methods and compositions for controlling the viscosity of viscoelastic surfactant fluids

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GB2058750A (en) 1981-04-15
IT1141046B (en) 1986-10-01
NL8003501A (en) 1981-03-17
BR8004199A (en) 1981-03-31
IT8024638A0 (en) 1980-09-12
DE3034721A1 (en) 1981-04-02
CA1140120A (en) 1983-01-25
AU5879280A (en) 1981-03-19

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